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- 2022
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Mark
Diagnosis and management of severe congenital protein C deficiency (SCPCD) : Communication from the SSC of the ISTH
- Contribution to journal › Article
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Mark
Thrombotic risk determined by rare and common SERPINA1 variants in a population-based cohort study
- Contribution to journal › Article
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Mark
Hereditary angioedema is associated with an increased risk of venous thromboembolism
- Contribution to journal › Letter
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Mark
Thrombomodulin (THBD) gene variants and thrombotic risk in a population-based cohort study
- Contribution to journal › Article
- 2021
-
Mark
Thrombocytopenia with acute ischemic stroke and bleeding in a patient newly vaccinated with an adenoviral vector-based COVID-19 vaccine : COMMENT from Gruel et al.: RESPONSE from Kahn et al.
- Contribution to journal › Letter
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Mark
The Copenhagen founder variant GP1BA c.58T>G is the most frequent cause of inherited thrombocytopenia in Denmark
- Contribution to journal › Article
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Mark
Suggested treatment of serious complications to COVID-19 vaccination with IdeS, a bacterial antibody-cleaving enzyme
- Contribution to journal › Letter
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Mark
Megakaryocytes listen for their progeny’s progeny during inflammation
- Contribution to journal › Debate/Note/Editorial
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Mark
Pleiotropic anticoagulant functions of protein S, consequences for the clinical laboratory. Communication from the SSC of the ISTH
- Contribution to journal › Article
-
Mark
Droplet digital PCR and mile-post analysis for the detection of F8 int1h inversions
- Contribution to journal › Article
